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Elisabetta Gazzerro

Showing results (31-40 of 50) with videos related to

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Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Stem Cell Research|January 6, 2018
Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 geneViviana Meraviglia, Patrizia Benzoni, Sara Landi, et al.
Biochemical and Biophysical Research Communications|November 14, 2012
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 geneChiara Fiorillo, Giacomo Brisca, Denise Cassandrini, et al.
Nature Communications|September 29, 2018
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophyFabio A Iannotti, Ester Pagano, Ombretta Guardiola, et al.
EMBO Molecular Medicine|January 3, 2023
Targeting gut dysbiosis against inflammation and impaired autophagy in Duchenne muscular dystrophyHilal Kalkan, Ester Pagano, Debora Paris, et al.
International Journal of Molecular Sciences|January 23, 2024
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 MutationsPatrizia Benzoni, Elisabetta Gazzerro, Chiara Fiorillo, et al.
Acta Neuropathologica Communications|April 13, 2018
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonismRasha Al-Khalidi, Chiara Panicucci, Paul Cox, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Stem Cell Research|January 6, 2018
Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 geneViviana Meraviglia, Patrizia Benzoni, Sara Landi, et al.
Biochemical and Biophysical Research Communications|November 14, 2012
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 geneChiara Fiorillo, Giacomo Brisca, Denise Cassandrini, et al.
Nature Communications|September 29, 2018
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophyFabio A Iannotti, Ester Pagano, Ombretta Guardiola, et al.
EMBO Molecular Medicine|January 3, 2023
Targeting gut dysbiosis against inflammation and impaired autophagy in Duchenne muscular dystrophyHilal Kalkan, Ester Pagano, Debora Paris, et al.
International Journal of Molecular Sciences|January 23, 2024
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 MutationsPatrizia Benzoni, Elisabetta Gazzerro, Chiara Fiorillo, et al.
Acta Neuropathologica Communications|April 13, 2018
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonismRasha Al-Khalidi, Chiara Panicucci, Paul Cox, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Pageof 5